Rosenthal K L, Zinkernagel R M
J Immunol. 1981 Feb;126(2):446-51.
H-2k mice are unable to generate cytotoxic T lymphocytes (CTL) to vesicular stomatitis virus (VSV). This apparent unresponsiveness is found for both major serotypes of VSV, VSV-Indiana and VSV-New Jersey. CTL unresponsiveness occurs despite the ability of H-2k mice to generate a humoral immune response against VSV that is comparable to that found in responder (H-2b and H-2a) strains. All H-2k mice regardless of background genes, including various Ig allotypes, were found to be nonresponders. H-2k-linked unresponsiveness mapped to both H-2Kk and H-2Dk and occurred despite the presence of responder alleles in (responder x nonresponder)F1 mice. The unresponsiveness cannot be attributed to an inability of VSV-infected H-2k target cells to express viral surface antigens of H-2 molecules. Further, unresponsiveness cannot be overcome by using secondary stimulation in vivo or in vitro. H-2k-linked unresponsiveness does not appear to be due to suppression, and no complementation has been found in various (nonresponder x nonresponder)F1 mice. Thus unresponsiveness to VSV in association with H-2Kk or H-2Dk appears to represent an extensive defect of immune responsiveness that probably occurs because VSV is not a natural mouse pathogen.
H-2k小鼠无法产生针对水疱性口炎病毒(VSV)的细胞毒性T淋巴细胞(CTL)。对于VSV的两种主要血清型,即VSV-印第安纳株和VSV-新泽西株,均发现了这种明显的无反应性。尽管H-2k小鼠能够产生针对VSV的体液免疫反应,且该反应与应答者(H-2b和H-2a)品系中的反应相当,但仍出现了CTL无反应性。所有H-2k小鼠,无论其背景基因如何,包括各种免疫球蛋白同种异型,均被发现为无反应者。与H-2k相关的无反应性定位于H-2Kk和H-2Dk,并且即使在(应答者×无反应者)F1小鼠中存在应答者等位基因时也会发生。这种无反应性不能归因于VSV感染的H-2k靶细胞无法表达H-2分子的病毒表面抗原。此外,体内或体外的二次刺激均无法克服这种无反应性。与H-2k相关的无反应性似乎并非由于抑制作用,并且在各种(无反应者×无反应者)F1小鼠中未发现互补现象。因此,与H-2Kk或H-2Dk相关的对VSV的无反应性似乎代表了免疫反应性的广泛缺陷,这可能是因为VSV不是天然的小鼠病原体。